Comparison of the mean effect of Remifentanil, Methadone, and Sufentanil on Pain and Delirium in Patients with spinal surgery
Phase 3
Recruiting
- Conditions
- multiple fractures of spine, level unspecified.Fracture of spine, level unspecified
- Registration Number
- IRCT20221218056854N1
- Lead Sponsor
- Ilam University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Patients with spinal surgery taking Remifentanil
Patients with spinal surgery taking Sufentanil
Patients with spinal surgery taking Methadone
Exclusion Criteria
Patients with Psychological History
Patients with History of Drug Addiction
Patients with History of Allergic Reaction to Drugs
Patients with History of Diabetes
Patients with History of Kidney Disease
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Delirium Severity and Duration. Timepoint: After Spinal Surgery, 6, 12, and 24 Hours After Surgery. Method of measurement: Physical Examination.;Four Main Delirium Features. Timepoint: After Spinal Surgery, 6, 12 and 24 Hours After Surgery. Method of measurement: CAM-ICU(Confusion Assessment Method for the Intensive Care Unit) Questionnaire.;Pain Intensity Score. Timepoint: After Spinal Surgery, 6, 12 and 24 Hours After Surgery. Method of measurement: Visual Analog Scale.
- Secondary Outcome Measures
Name Time Method